203631-76-9

Basic information

• Product Name: 4-[4-(4-Isopropoxy-phenylsulfanyl)-phenylsulfanyl]-benzenethiol
• Synonyms: 4-[4-(4-Isopropoxy-phenylsulfanyl)-phenylsulfanyl]-benzenethiol
• CAS NO: 203631-76-9
• Molecular Weight: 384.587
• Mol File: 203631-76-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-[4-(4-Isopropoxy-phenylsulfanyl)-phenylsulfanyl]-benzenethiol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[4-(4-Isopropoxy-phenylsulfanyl)-phenylsulfanyl]-benzenethiol(203631-76-9)
• EPA Substance Registry System: 4-[4-(4-Isopropoxy-phenylsulfanyl)-phenylsulfanyl]-benzenethiol(203631-76-9)

Safety Data

• Hazardous Substances Data: 203631-76-9(Hazardous Substances Data)

Upstream product

• 203631-77-0 C₁₆H₁₈OS₂ 
• 203631-75-8 4-(4-Isopropoxy-phenylsulfanyl)-benzenethiol 
• 33932-80-8 4-(methylthio)phenyl phenyl sulfide 
• 104-95-0 (4-bromophenyl)thioanisole 
• 100-68-5 methyl-phenyl-thioether 
• 203631-72-5 1-methylsulfanyl-4-(4-bromophenylsulfanyl)-benzene 
• 702-12-5 4-isopropyloxythiophenol 
• 203631-79-2 C₂₂H₂₂OS₃ 

Relevant articles and documents

Efficient formation of aromatic thiols from thiomethylated precursors

As a model study, a series of linear and branched p-phenylene and m- phenylene sulfides, functionalized by a thiomethyl group, were deprotected to thiols while using various alkyl thiolates at 160°C in DMF. Many complex aromatic thiols were obtained in al

Synthesis of p-phenylene sulfide molecular asterisks

'Megastars' with aromatic central cores, some of which fluoresce, were synthesized by the efficient connection of the side arms to the core by using the MacNicol reaction. Depending on the length of the side arm precursor, second-, third- (depicted), or f